US20040209891A1 - Treatment of type 2 diabetes with inhibitors of dipeptidyl peptidase IV - Google Patents

Treatment of type 2 diabetes with inhibitors of dipeptidyl peptidase IV Download PDF

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US20040209891A1
US20040209891A1 US10/474,676 US47467604A US2004209891A1 US 20040209891 A1 US20040209891 A1 US 20040209891A1 US 47467604 A US47467604 A US 47467604A US 2004209891 A1 US2004209891 A1 US 2004209891A1
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inhibitor
dipeptidyl peptidase
prodrug
diabetes
use according
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Pierre Broqua
Beatrice Sudre
Michael Aubert
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Ferring BV
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Ferring BV
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Assigned to FERRING BV reassignment FERRING BV ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BROQUA, PIERRE, AUBERT, MICHEL L., SUDRE, BEATRICE
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/426—1,3-Thiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Definitions

  • the present invention relates to a method for delaying the onset of type 2 diabetes and alleviating the physiological consequences of type 2 diabetes.
  • Type 2 diabetes also known as non-insulin dependent diabetes mellitus, accounts for more than 80% of all cases.
  • Type 2 diabetes is particularly prevalent in obese people aged over 40.
  • Complications of type 2 diabetes include retinopathy and nephropathy, and diabetics have a significantly increased chance of suffering cardiovascular disease.
  • a number of drugs are available for the treatment of type 2 diabetes, but new ones, particularly those acting by novel mechanisms, are still needed.
  • One such class of candidate therapeutic agents comprises inhibitors of dipeptidyl peptidase IV (DP-IV, EC.3.4.14.5). These compounds act, at least in part, by blocking the inactivation of endogenous incretins such as GLP-1 and GIP, resulting in an increased sensitivity to insulin and reduced post-prandial hyperglycaemia. To date, however, these compounds have only been examined as a method for controlling the management of blood glucose levels on an acute basis. The implications of long-term treatment with these compounds have not been considered.
  • one aspect of the present invention is a method of treating individuals at risk of developing type 2 diabetes, or in the early stages thereof, so as to prevent the progression of the disease, which method is to administer to the said individual repeated doses of a pharmaceutical composition comprising an inhibitor of DP-IV.
  • Another aspect of the invention is a pharmaceutical composition for use in such treatment.
  • a third aspect of the present invention is the use of inhibitors of DP-IV to prepare such compositions.
  • ZDF Zucker Diabetic Fatty
  • DP-IV DP-IV
  • the ZDF rat is a well known model for human type 2 diabetes.
  • ZDF rats are hyperphagic, and when fed on a high fat diet they become diabetic, as shown by hyperglycaemia, hypertrigyceridaemia, polydipsia and an increase in circulating free fatty acids.
  • Disease onset is observed at about 8 weeks and the animals are fully diabetic by 11 weeks of age.
  • chronic treatment of ZDF rats with inhibitors of DP-IV leads to a significant delay in the onset of the diabetic state, which indicates that such chronic treatment will be useful in human subjects at risk of developing type 2 diabetes, or in the early stages of the disease.
  • a first aspect of the present invention is a method of treating an individual at risk of developing type 2 diabetes, or in the early stages thereof, so as to delay the onset and progression of the disease.
  • the treatment comprises the administration to the said individual of repeated doses of an inhibitor of DP-IV.
  • the assessment that an individual is at risk of developing type 2 diabetes will generally be made by an experienced physician, who will take into consideration such factors as the age and weight (and more specifically the body mass index, BMI) of the individual, as well as any history of diabetes in the individual's family and other risk factors. Similarly, a diagnosis of early-stage type 2 diabetes will be made by an experienced physician on the basis of a number of standard analyses and tests.
  • the inhibitor of DP-IV may be any compound that inhibits the enzymatic activity of DP-IV at a pharmacologically relevant dose.
  • Suitable compounds can be identified as those that significantly inhibit the enzymatic activity of DP-IV in an in vitro assay at concentrations below 10 ⁇ M.
  • Particularly suitable compounds are those that inhibit the enzymatic activity of DP-IV at concentrations below 0.1 ⁇ M. Such activity can be easily determined by one skilled in the art using one of the published assays.
  • Suitable compounds should in addition preferably be selective, i.e.
  • prodrugs of DP-IV inhibitors are well known in the art.
  • a prodrug is a compound that is generally inactive per se, but which is subject to chemical or metabolic modification after administration, which modification causes the release of the active pharmaceutical agent.
  • Prodrugs are typically used to increase oral bioavailability or to prolong the duration of action of a compound.
  • the inhibitor of DP-IV is an ⁇ -aminoacyl pyrrolidide, an ⁇ -aminoacyl thiazolidide, an ⁇ -aminoacyl pyrrolidinenitrile, or an ⁇ -aminoacyl thiazolidinenitrile.
  • the inhibitor of DP-IV is a compound according to general formula 1 or general formula 2, or a pharmaceutically acceptable salt of either of these.
  • X is selected from a methylene group CH 2 and a sulphur atom S;
  • R 1 is selected from C 1 -C 6 alkyl groups, including branched and cyclic alkyl groups, and (CH 2 ) n R 3 ;
  • R 2 is selected from a hydrogen atom H and a nitrile group CN;
  • R 3 is selected from NH-Het and NHCO-Het;
  • Het is a pyridyl, pyrimidyl or pyrazinyl group that is optionally substituted with up to two groups independently selected from methyl, Cl, F, CN and CF 3 ; and
  • n is 2, 3, 4 or 5.
  • the compounds according to general formulae 1 and 2 all have at least one basic nitrogen atom and so are able to form addition salts with protic acids.
  • examples of such acids include hydrochloric acid, sulphuric acid, phosphoric acid, acetic acid, trifluoroacetic acid, fumaric acid, maleic acid, citric acid, benzoic acid, pamoic acid and methanesulphonic acid.
  • these acids are pharmaceutically acceptable, such salts are included within the scope of the present invention.
  • the compounds according to general formula 1 have a stereogenic centre (asymmetric carbon atom) in the aminoacyl group.
  • R 2 is a nitrile
  • the compounds according to both general formulae have a stereogenic centre in the five-membered ring. Accordingly, these compounds can exist as optical isomers such as enantiomers and diastereomers. All such isomers are included within the scope of the present invention.
  • the preferred stereochemistry is that illustrated in general formulae 3 and 4.
  • the inhibitor is a compound according to general formula 1. More preferably, it is a compound according to general formula 1 wherein R 1 is a C 4 branched alkyl group such as sec-butyl or tert-butyl. Most preferably it is such a compound wherein X is CH 2 and R 2 is a nitrile, or X is S and R 2 is H.
  • the inhibitor is a compound according to general formula 2. More preferably, it is a compound according to general formula 2 wherein R 1 is (CH 2 ) n R 3 , n is 2 and R 3 is NH-Het. Most preferably it is such a compound wherein X is CH 2 , R 2 is a nitrile, and Het is 5-cyano-2-pyridyl.
  • the inhibitor of DP-IV will be administered to the individual as a pharmaceutical composition such as, for example, a tablet, capsule, powder, suppository, solution or suspension.
  • a pharmaceutical composition such as, for example, a tablet, capsule, powder, suppository, solution or suspension.
  • the general principles for the preparation of such formulations are well known in the art.
  • the formulation may further comprise such pharmaceutically acceptable excipients as bulking agents, binding agents, preservatives, solvents, flavoring agents and the like. It may further include one or more additional pharmacologically active agents, such as anti-diabetic agents, but preferably the DP-IV inhibitor is the sole active agent.
  • the formulation may be administered by any appropriate route, including oral, buccal, sublingual, rectal, intravaginal and transdermal administration as well as by intravenous, subcutaneous and intramuscular injection.
  • the formulation is administered orally as a tablet or capsule.
  • the dose will be determined by the attending physician, taking into consideration all the relevant factors. Typically a single dose will comprise between 1 mg and 1000 mg, preferably between 5 mg and 250 mg. The dose may be given once per day or more often, such as twice or three times per day. Treatment will be continued for an extended period of time such as several weeks, months or even years.
  • the formulation may be administered as a depot which releases active compound over a period of between one week and three months.
  • controlled-release formulations are known in the art, and generally comprise a pharmaceutically active species associated with a biocompatible polymer.
  • the polymer may simply encapsulate the active agent, forming a physical barrier to its release into the general circulation, or there may be a chemical association, such as a covalent or ionic interaction, between the polymer and the active agent.
  • Such formulations are generally administered by intramuscular or subcutaneous injection. In this case, the administration will be repeated at intervals of one week up to three months so as to maintain treatment over an extended period.
  • a second aspect of the present invention is a pharmaceutical composition for the treatment of a person at risk of developing type 2 diabetes, or in the early stages thereof, so as to delay or prevent the progression of the disease.
  • the composition comprises an inhibitor of DP-IV as described above, suitably formulated, together with instructions for repeated dosing.
  • a third aspect of the present invention is the use of an inhibitor of DP-IV for the preparation of a pharmaceutical composition for the treatment of a person at risk of developing type 2 diabetes, or in the early stages thereof, so as to delay or prevent the progression of the disease.
  • Inhibitors of DP-IV can be prepared according to published methods.
  • the title compound is prepared according to the methods of WO95/15309, and particularly of Example 13 therein. Briefly, BOC-protected tert-butylglycine is coupled to prolineamide, the primary amide function is dehydrated with trifluoroacetic anhydride to give the nitrile and the BOC-group is removed with HCl in dioxan.
  • N ⁇ -BOC-protected N ⁇ -pyrazinecabonylornithine is coupled to prolineamide, the primary amide function is dehydrated with trifluoroacetic anhydride to give the nitrile, and the BOC-group is removed with trifluoroacetic acid.
  • the title compound is prepared according to the standard methods. Briefly, BOC-protected isoleucine is coupled to thiazolidine and the BOC-group is removed with HCl in dioxan.
  • the title compound is prepared according to the methods of WO98/19998, and particularly of Example 3 therein. Briefly, bromoacetyl bromide is reacted with prolineamide and the product is dehydrated with trifluoroacetic anhydride to give N-bromoacetylpyrrolidine-2-carbonitrile. This is treated with 2-(5-cyano-2-pyridylamino)ethylamine to give the product.
  • Example 1A Male ZDF rats, aged 6.5 weeks at the beginning of the study (day 0), are given the compound of Example 1A (10 mg/kg p.o.) once or twice per day for four weeks. Control animals are given vehicle. A group of untreated lean rats is used as a comparison. Glycaemia, insulinaemia, body weight, food and water intake, and plasma triglyceride and free fatty acid levels are monitored throughout the study.
  • Plasma free fatty acid and triglyceride levels are significantly elevated in the obese animals at day 0, and in control obese animals they increase throughout the study period. Once-daily, and particularly twice-daily treatment attenuates this increase. The results are presented in FIGS. 6 and 7.

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  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Diabetes (AREA)
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  • Engineering & Computer Science (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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US10/474,676 2001-04-11 2002-04-10 Treatment of type 2 diabetes with inhibitors of dipeptidyl peptidase IV Abandoned US20040209891A1 (en)

Applications Claiming Priority (3)

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GBGB0109146.1A GB0109146D0 (en) 2001-04-11 2001-04-11 Treatment of type 2 diabetes
GB0109146.1 2001-04-11
PCT/GB2002/001674 WO2002083109A1 (en) 2001-04-11 2002-04-10 Treatment of type 2 diabetes with inhibitors of dipeptidyl peptidase iv

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EP (1) EP1377278B1 (de)
JP (1) JP2004525179A (de)
KR (1) KR20040025915A (de)
CN (1) CN1248683C (de)
AT (1) ATE344029T1 (de)
AU (1) AU2002244860B2 (de)
CA (1) CA2443229A1 (de)
CZ (1) CZ20032927A3 (de)
DE (1) DE60215787T2 (de)
GB (1) GB0109146D0 (de)
HK (1) HK1059213A1 (de)
HU (1) HUP0303876A3 (de)
IL (1) IL157821A0 (de)
MX (1) MXPA03009224A (de)
NO (1) NO20034549D0 (de)
NZ (1) NZ528172A (de)
PL (1) PL366633A1 (de)
RU (1) RU2328283C2 (de)
UA (1) UA76452C2 (de)
WO (1) WO2002083109A1 (de)
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US7723344B2 (en) 2003-08-13 2010-05-25 Takeda San Diego, Inc. Dipeptidyl peptidase inhibitors
US7732446B1 (en) 2004-03-11 2010-06-08 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
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US7790734B2 (en) 2003-09-08 2010-09-07 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
US7825242B2 (en) 2004-07-16 2010-11-02 Takeda Pharmaceutical Company Limted Dipeptidyl peptidase inhibitors
US7872124B2 (en) 2004-12-21 2011-01-18 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
US7960384B2 (en) 2006-03-28 2011-06-14 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
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US8084605B2 (en) 2006-11-29 2011-12-27 Kelly Ron C Polymorphs of succinate salt of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethy]-4-fluor-benzonitrile and methods of use therefor
US8093236B2 (en) 2007-03-13 2012-01-10 Takeda Pharmaceuticals Company Limited Weekly administration of dipeptidyl peptidase inhibitors
US8222411B2 (en) 2005-09-16 2012-07-17 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
US8324383B2 (en) 2006-09-13 2012-12-04 Takeda Pharmaceutical Company Limited Methods of making polymorphs of benzoate salt of 2-[[6-[(3R)-3-amino-1-piperidinyl]-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl]methyl]-benzonitrile
US8906901B2 (en) 2005-09-14 2014-12-09 Takeda Pharmaceutical Company Limited Administration of dipeptidyl peptidase inhibitors
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US11253508B2 (en) 2017-04-03 2022-02-22 Coherus Biosciences, Inc. PPARy agonist for treatment of progressive supranuclear palsy

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GB0526291D0 (en) 2005-12-23 2006-02-01 Prosidion Ltd Therapeutic method
PE20071221A1 (es) 2006-04-11 2007-12-14 Arena Pharm Inc Agonistas del receptor gpr119 en metodos para aumentar la masa osea y para tratar la osteoporosis y otras afecciones caracterizadas por masa osea baja, y la terapia combinada relacionada a estos agonistas
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US10894787B2 (en) 2010-09-22 2021-01-19 Arena Pharmaceuticals, Inc. Modulators of the GPR119 receptor and the treatment of disorders related thereto
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WO2018162722A1 (en) 2017-03-09 2018-09-13 Deutsches Institut Für Ernährungsforschung Potsdam-Rehbrücke Dpp-4 inhibitors for use in treating bone fractures

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AU2002244860B2 (en) 2006-11-16
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CZ20032927A3 (cs) 2004-06-16
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